Helmut Klein, Angelo Auricchio,
Christoph J. Geller, Hans-Dieter Esperer, Sven Reek, Wolfgang Hartung.
Division of Cardiology, University Hospital, Otto-von-Guericke Universität,
Magdeburg, Germany
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Until a few years ago antiarrhythmic drugs,
electrophysiologically guided surgery, catheter ablation and implantation of the automatic
defibrillator were competing approaches for the treatment of life-threatening ventricular
tachyarrhythmias1. Today, however, EP-guided surgery
and catheter ablation have lost their role in the prevention of sudden arrhythmic death
and the results of drug trials like CAST, SWORD, EMIAT2
and CAMIAT have raised doubt whether antiarrhythmic drugs are able to prevent sudden
cardiac death (SCD) or reduce overall or cardiac mortality in a patient population prone
to life-threatening ventricular tachyarrhythmias. The implantable defibrillator,
contrarily, has impressively established its role in the treatment of ventricular
tachycardia and ventricular fibrillation3,4.
Until today there is no other approach than ICD treatment that is able to reduce
sudden cardiac death to about 2% within two years after a serious arrhythmic event. The
beneficial effect of the ICD for secondary prevention of SCD has been demonstrated in the
large AVID trial. There was a 38% reduction in overall mortality at 1 year and a 25%
decrease at two and three years respectively in comparison with amiodarone or sotalol. We
are awaiting the results of two other major secondary prevention trials, the CASH and CIDS
studies which also compare ICD treatment with amiodarone. But even if these two studies
will demonstrate no ICD benefit it is highly unlikely that amiodarone will be more
favorable than ICD treatment. Today, as well as tomorrow, it will be hard to deny that
primary treatment for secondary prevention of SCD is other than ICD implantation and there
is hardly justification for further SCD secondary prevention trials.
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